반응 #87085

ord-f425c6a51d364bb0967b957e504c943b

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과filtered through a pad of celite
  2. 2
    농축The filtrate was concentrated under reduced pressure
  3. 3
    세척the residue was washed with EtOAc (10 mL)

실험 절차

To a solution of (2S,3R)-benzyl 3-hydroxy-3-(4-methoxyphenyl)-2-((S)-2-(2-morpholino acetamido)propanamido)propanoate (2.0 g, 4.0 mmol) in THF (40 mL) was added Pd/C (500 mg, 10%). The mixture was stirred under a hydrogen atmosphere (1 atm) at ambient temperature overnight and then filtered through a pad of celite. The filtrate was concentrated under reduced pressure and the residue was washed with EtOAc (10 mL) to afford (2S,3R)-3-hydroxy-3-(4-methoxyphenyl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanoic acid (1.30 g, 78% yield) as a colorless solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09434761B2uspto-grants-2016_09